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Arterial lesions in Behçet's disease
D Saba1, H Saricaoğlu, A S Bayram
1Uludağ University Medical Faculty, Department of Thoracic and Cardiovascular Surgery, Göğüs, Kalp ve Damar Cerrahisi Ana Bilim Dali, Görükle, 16059, Bursa, Turkey. davids@uludag.edu.tr
Insights
Behçet's disease arterial lesions, especially pulmonary artery aneurysms, show poor prognosis. Corticosteroids effectively treat non-pulmonary arterial occlusive disease, while aneurysms require surgery or stent-grafts.
Area of Science:
- Vascular Medicine
- Rheumatology
- Immunology
Background:
- Arterial involvement is a rare but serious complication of Behçet's disease.
- This study assesses therapeutic outcomes for arterial lesions in Behçet's disease patients.
Purpose of the Study:
- To evaluate the effectiveness of various treatments for arterial lesions in Behçet's disease.
- To determine the prognosis of pulmonary artery aneurysms and non-pulmonary arterial lesions in Behçet's disease.
Main Methods:
- Retrospective evaluation of 534 Behçet's disease patients diagnosed between 1987 and 2002.
- Follow-up intervals of 3 to 6 months to monitor arterial lesions.
- Analysis of therapeutic interventions including surgery, stent-graft insertion, and immunosuppressive therapy.
Main Results:
- Arterial lesions were found in 21 patients (3.9%).
- Pulmonary artery aneurysms (PAA) had a high mortality rate, with all three surgically treated patients dying. Survivors received cyclophosphamide and corticosteroids.
- Non-pulmonary arterial lesions were treated with surgery or stent-grafts; one patient died 8 years post-intervention. Corticosteroids were successful for occlusive lesions.
Conclusions:
- Pulmonary artery aneurysms in Behçet's disease carry a poor prognosis regardless of treatment.
- High-dose corticosteroids are effective for isolated non-pulmonary arterial occlusive lesions.
- Surgery or stent-graft insertion is recommended for non-pulmonary arterial aneurysms due to high complication risks.
Background:
Arterial involvement is a rare but serious condition in the course of Behçet's disease. We aimed to assess the results of therapeutic approaches in our patients with arterial lesions caused by Behçet's disease.
Patients And Methods:
The records of 534 patients with Behçet's disease between 1987 and 2002 were retrospectively evaluated for the presence of arterial lesions. All patients were followed up regularly at 3 to 6 months intervals.
Results:
Arterial lesions were diagnosed in 21 (3.9%) patients. Eight of these patients had pulmonary artery aneurysms (PAA), and the other 13 patients had non-pulmonary arterial lesions. Urgent surgical intervention was performed in three patients with PAA leading to death in all three. In addition, three other patients died due to massive haemoptysis at home despite to immunosuppressive therapy. Only two out of eight patients with PAA are still alive who were treated with cyclophophamide and corticosteroids. Thirteen operations were performed in 7 out of 13 patients having non-pulmonary arterial lesions. Although ten of the operations were primary operations, three reoperations had to be performed. A stent-graft was applied for the management of an iliac artery aneurysm in one patient. Only one patient died 8 years after the first non-pulmonary arterial involvement following a type IV thoracoabdominal aortic aneurysm repair. Five patients with arterial occlusive lesions were successfully treated by corticosteroids.
Conclusions:
Pulmonary artery aneurysms in Behçet's disease patients have a poor prognosis despite any form of therapy. High dose corticosteroids alone can be successfully used for isolated non-pulmonary arterial occlusive lesions, unless disabling symptoms occur. Surgery or stent-graft insertion is indicated for non-pulmonary arterial aneurysms because these aneurysms entail high risk of complications.
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